Science · 2011 · 888 citations · 23 references
Life SciencesCell BiologyHematologyCell TherapyStem Cell BiologyStem Cell TransplantationBlood Cell DifferentiationHematopoietic DevelopmentHematopoietic DifferentiationHematopoietic Stem Cell BiologyHematopoietic Stem Cell TransplantationHematopoietic Stem CellsHematopoietic Stem Cell EnrichmentHematopoietic Stem Cell IsolationHematopoietic Stem Cell MaintenanceMultipotent Progenitor CellsMultipotent ProgenitorsPurificationStem Cell-based Therapy
Lifelong blood cell production is dependent on rare hematopoietic stem cells (HSCs) to perpetually replenish mature cells via a series of lineage-restricted intermediates. Investigating the molecular state of HSCs is contingent on the ability to purify HSCs away from transiently engrafting cells. We demonstrated that human HSCs remain infrequent, using current purification strategies based on Thy1 (CD90) expression. By tracking the expression of several adhesion molecules in HSC-enriched subsets, we revealed CD49f as a specific HSC marker. Single CD49f(+) cells were highly efficient in generating long-term multilineage grafts, and the loss of CD49f expression identified transiently engrafting multipotent progenitors (MPPs). The demarcation of human HSCs and MPPs will enable the investigation of the molecular determinants of HSCs, with a goal of developing stem cell-based therapeutics.
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Long-Term Lymphohematopoietic Reconstitution by a Single CD34-Low/Negative Hematopoietic Stem Cell
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